作者
Shihang Pu,Shijie Qian,Yiheng Ding,Qi Li,Baochao Li,Jiajun Xing,Ling Jin,Xiaohai Xi,Zengjun Wang,Aiming Xu,Tao Wang
摘要
BACKGROUND: Sunitinib resistance remains a major clinical challenge in renal cell carcinoma, and the underlying molecular mechanisms are incompletely understood. SP5, a member of the specificity protein transcription factor family, has been implicated in tumor progression, but its role in sunitinib resistance and angiogenesis in RCC is unclear. METHODS: We integrated bulk RNA-seq datasets (GSE172165, GSE173572, GSE216494) and single-cell transcriptomics (GSE156632) to identify sunitinib resistance-associated differentially expressed genes. A prognostic model was constructed using 117 machine-learning algorithms and validated across multiple independent cohorts. Functional assays, including CCK-8, colony formation, transwell, tube formation, CUT&RUN, and xenograft models, were performed. Virtual screening and molecular docking identified suramin as a potential SP5 inhibitor. RESULTS: We identified SP5 as a core resistance-related gene. The risk model effectively stratified patients, with high-risk individuals showing worse prognosis, elevated TMB, and immunosuppressive microenvironments. Mechanistically, SP5 directly bound to the VEGFA promoter to upregulate VEGFA transcription, activating AKT phosphorylation via autocrine and paracrine loops, thereby promoting angiogenesis and sunitinib resistance. SP5 knockdown suppressed proliferation, migration, invasion, and tube formation, and resensitized cells to sunitinib. Suramin disrupted the SP5-VEGFA interaction, synergized with sunitinib to inhibit tumor growth, and reduced VEGFA secretion. CONCLUSION: Our findings establish SP5 as a critical driver of sunitinib resistance and identify suramin as a promising therapeutic strategy.